免疫系统
Toll样受体
细胞生物学
过继性细胞移植
功能(生物学)
生物
信号转导
受体
Treg细胞
树突状细胞
免疫学
调节性T细胞
T细胞
癌症研究
先天免疫系统
白细胞介素2受体
遗传学
作者
Guangyong Peng,Zhong Guo,Yukiko Kiniwa,Kui Shin Voo,Weiyi Peng,Tihui Fu,Daniel Wang,Yanchun Li,Helen Y. Wang,Rongfu Wang
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2005-08-25
卷期号:309 (5739): 1380-1384
被引量:734
标识
DOI:10.1126/science.1113401
摘要
CD4+ regulatory T (Treg) cells have a profound ability to suppress host immune responses, yet little is understood about how these cells are regulated. We describe a mechanism linking Toll-like receptor (TLR) 8 signaling to the control of Treg cell function, in which synthetic and natural ligands for human TLR8 can reverse Treg cell function. This effect was independent of dendritic cells but required functional TLR8-MyD88-IRAK4 signaling in Treg cells. Adoptive transfer of TLR8 ligand-stimulated Treg cells into tumor-bearing mice enhanced anti-tumor immunity. These results suggest that TLR8 signaling could play a critical role in controlling immune responses to cancer and other diseases.
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